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Diskom

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref DKR1908CDFL10

by Biopsybell Srl

Identity

Trade Name
DISKOM EUDAMED
BIOPSYBELL FDA UDI
Generic Name
Diskectomy system, percutaneous, automatic FDA UDI
Device Name
DISCECTOMY SYSTEMS EUDAMED
DISKOM EUDAMED
DISC DECOMPRESSION NEEDLE FDA UDI
Model / Reference
DKR1908CDFL10 EUDAMED
DISKOM FDA UDI
Description
DISC DECOMPRESSION NEEDLE FDA UDI

Identifiers

Catalog Number
DKR1908CDFL10 FDA UDI
Primary DI / UDI-DI
08033860019747 EUDAMEDFDA UDI
Basic UDI-DI
8033860DISCFT01D77 EUDAMED
B-08033860019747 EUDAMED
510(k) Number
K180315 FDA UDI
FDA Product Code
HRX FDA UDI
EMDN Code
A01020102 ASPIRATION FINE NEEDLES AND KITS EUDAMED
GMDN Term
Diskectomy system, percutaneous, automatic FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 80 Millimeter FDA UDI
Needle Gauge — 19 Gauge FDA UDI

Category: Diskectomy system, percutaneous, automatic

Diskom by Biopsybell Srl — Class IIa — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diskectomy system, percutaneous, automatic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (3)

  • EUDAMED 1ec02f44-9301-4f66-a189-25efd03c0eab 61 fields · synced Jul 11, 2026
  • FDA UDI e46c4489-4c0d-4fef-bf54-a907314b6854 37 fields · synced May 30, 2026
  • EUDAMED d9ccc25f-0c2f-4aea-9e5b-24409a806a71 61 fields · synced Jun 19, 2026